HK1114851A1 - Polycyclic indazole derivatives that are erk inhibitors - Google Patents
Polycyclic indazole derivatives that are erk inhibitorsInfo
- Publication number
- HK1114851A1 HK1114851A1 HK08110160.5A HK08110160A HK1114851A1 HK 1114851 A1 HK1114851 A1 HK 1114851A1 HK 08110160 A HK08110160 A HK 08110160A HK 1114851 A1 HK1114851 A1 HK 1114851A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- indazole derivatives
- erk inhibitors
- polycyclic
- polycyclic indazole
- erk
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US74985605P | 2005-12-13 | 2005-12-13 | |
PCT/US2006/046959 WO2007070398A1 (en) | 2005-12-13 | 2006-12-11 | Polycyclic indazole derivatives that are erk inhibitors |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1114851A1 true HK1114851A1 (en) | 2008-11-14 |
Family
ID=37969564
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK08110160.5A HK1114851A1 (en) | 2005-12-13 | 2008-09-12 | Polycyclic indazole derivatives that are erk inhibitors |
Country Status (29)
Country | Link |
---|---|
US (1) | US20070191604A1 (en) |
EP (1) | EP1966151B1 (en) |
JP (1) | JP4881957B2 (en) |
KR (1) | KR101417136B1 (en) |
CN (1) | CN101370784B (en) |
AR (1) | AR056891A1 (en) |
AT (1) | ATE527240T1 (en) |
AU (1) | AU2006326616B2 (en) |
BR (1) | BRPI0619823B8 (en) |
CA (1) | CA2633023C (en) |
CY (1) | CY1112760T1 (en) |
DK (1) | DK1966151T3 (en) |
EC (1) | ECSP088550A (en) |
ES (1) | ES2372976T3 (en) |
HK (1) | HK1114851A1 (en) |
HR (1) | HRP20110892T1 (en) |
IL (1) | IL192034A (en) |
MY (1) | MY149430A (en) |
NO (1) | NO341831B1 (en) |
NZ (1) | NZ569087A (en) |
PE (2) | PE20100562A1 (en) |
PL (1) | PL1966151T3 (en) |
PT (1) | PT1966151E (en) |
RS (1) | RS51981B (en) |
RU (1) | RU2442778C9 (en) |
SI (1) | SI1966151T1 (en) |
TW (1) | TWI344466B (en) |
WO (1) | WO2007070398A1 (en) |
ZA (1) | ZA200805525B (en) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
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US8546404B2 (en) * | 2005-12-13 | 2013-10-01 | Merck Sharp & Dohme | Compounds that are ERK inhibitors |
DE602007009932D1 (en) * | 2006-02-16 | 2010-12-02 | Schering Corp | PYRROLIDIN DERIVATIVES AS ERK HEMMER |
KR20090042779A (en) | 2006-06-30 | 2009-04-30 | 쉐링 코포레이션 | Substituted piperidines that increase p53 activity and the uses thereof |
BRPI0812450A2 (en) * | 2007-06-05 | 2019-09-24 | Schering Corp | polycyclic indazole derivatives and their use as erk inhibitors for cancer treatment |
AR067354A1 (en) | 2007-06-29 | 2009-10-07 | Sunesis Pharmaceuticals Inc | USEFUL COMPOUNDS AS INHIBITORS OF RAF QUINASA |
MX2010005960A (en) * | 2007-11-30 | 2010-06-11 | Schering Corp | Braf biomarkers. |
CA2714479A1 (en) * | 2008-02-21 | 2009-08-27 | Schering Corporation | Compounds that are erk inhibitors |
AU2009222144A1 (en) | 2008-02-29 | 2009-09-11 | Array Biopharma Inc. | Pyrazole [3, 4-b] pyridine Raf inhibitors |
US20110278332A1 (en) * | 2009-03-26 | 2011-11-17 | Protexer, Inc. | Shoe cover removal apparatus |
US8637554B2 (en) * | 2008-05-07 | 2014-01-28 | The Trustees Of The University Of Pennsylvania | Methods for treating thyroid cancer |
US8586543B2 (en) * | 2008-08-19 | 2013-11-19 | Merck Sharp & Dohme Corp. | IL-8 biomarker for monitoring cancer treatment with certain ERK inhibitors |
US9229008B2 (en) | 2008-08-19 | 2016-01-05 | Merck Sharp & Dohme Corp. | IL-8 level as a determinant of responsivity of a cancer to treatment |
WO2011002887A1 (en) | 2009-07-02 | 2011-01-06 | Schering Corporation | FUSED TRICYCLIC COMPOUNDS AS NOVEL mTOR INHIBITORS |
US8658651B2 (en) | 2009-09-30 | 2014-02-25 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
PE20121172A1 (en) | 2009-10-14 | 2012-09-05 | Merck Sharp & Dohme | PIPERIDINS SUBSTITUTED WITH ACTIVITY IN HDM2 |
WO2011123937A1 (en) * | 2010-04-06 | 2011-10-13 | University Health Network | Kinase inhibitors and method of treating cancer with same |
EP2584903B1 (en) | 2010-06-24 | 2018-10-24 | Merck Sharp & Dohme Corp. | Novel heterocyclic compounds as erk inhibitors |
EP2608669B1 (en) | 2010-08-23 | 2016-06-22 | Merck Sharp & Dohme Corp. | NOVEL PYRAZOLO[1,5-a]PYRIMIDINE DERIVATIVES AS mTOR INHIBITORS |
EP2613782B1 (en) * | 2010-09-01 | 2016-11-02 | Merck Sharp & Dohme Corp. | Indazole derivatives useful as erk inhibitors |
EP2649065A1 (en) | 2010-12-09 | 2013-10-16 | Amgen Inc. | Bicyclic compounds as pim inhibitors |
EP2654748B1 (en) | 2010-12-21 | 2016-07-27 | Merck Sharp & Dohme Corp. | Indazole derivatives useful as erk inhibitors |
WO2012129338A1 (en) | 2011-03-22 | 2012-09-27 | Amgen Inc. | Azole compounds as pim inhibitors |
WO2012145471A1 (en) | 2011-04-21 | 2012-10-26 | Merck Sharp & Dohme Corp. | Insulin-like growth factor-1 receptor inhibitors |
US8901142B2 (en) | 2011-07-26 | 2014-12-02 | Merck Sharp & Dohme Corp. | Fused tricyclic compounds as mTOR inhibitors |
US8987274B2 (en) | 2011-10-28 | 2015-03-24 | Merck Sharp & Dohme Corp | Macrocycles that increase p53 activity and the uses thereof |
US9062071B2 (en) | 2011-12-21 | 2015-06-23 | Merck Sharp & Dohme Corp. | Substituted piperidines as HDM2 inhibitors |
WO2013109142A1 (en) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Combined pdk and mapk/erk pathway inhibition in neoplasia |
ITMI20120135A1 (en) * | 2012-02-02 | 2013-08-03 | Diab Int Ab | PROCEDURE FOR THE PRODUCTION OF PET FOAM AND PET FOAM OBTAINED WITH THIS PROCEDURE |
WO2013169858A1 (en) | 2012-05-08 | 2013-11-14 | The Broad Institute, Inc. | Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy |
CN103450163B (en) * | 2012-05-29 | 2017-06-23 | 中国医学科学院药物研究所 | Indazole compounds, its preparation method and its medicinal usage |
IN2015DN01328A (en) | 2012-09-19 | 2015-07-03 | Novartis Ag | |
AU2013323508B2 (en) * | 2012-09-28 | 2017-11-02 | Merck Sharp & Dohme Corp. | Novel compounds that are ERK inhibitors |
WO2014100065A1 (en) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as hdm2 inhibitors |
WO2015041534A1 (en) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk in combination with raf/erk/mek |
US9629851B2 (en) | 2013-09-20 | 2017-04-25 | Stitching Het Nederlands Kanker Institut—Antoni Van Leeuwenhoek Ziekenhuis | ROCK in combination with MAPK pathway |
SG11201601467SA (en) | 2013-11-01 | 2016-05-30 | Novartis Ag | Aminoheteroaryl benzamides as kinase inhibitors |
WO2015156674A2 (en) | 2014-04-10 | 2015-10-15 | Stichting Het Nederlands Kanker Instituut | Method for treating cancer |
WO2015178770A1 (en) | 2014-05-19 | 2015-11-26 | Stichting Het Nederlands Kanker Instituut | Compositions for cancer treatment |
WO2016095088A1 (en) | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
WO2016095089A1 (en) | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
US10864179B2 (en) | 2015-10-01 | 2020-12-15 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Histone deacetylase inhibitors for the use in the treatment of drug resistant melanoma |
JP6931646B2 (en) | 2015-10-21 | 2021-09-08 | 大塚製薬株式会社 | Benlactam compound |
WO2017099591A1 (en) | 2015-12-07 | 2017-06-15 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Treatment of inhibitor resistant braf-mutant cancers |
WO2017156495A1 (en) | 2016-03-11 | 2017-09-14 | Corvus Pharmaceuticals, Inc. | Compounds and methods for modulating bruton's tyrosine kinase |
WO2017204626A1 (en) | 2016-05-24 | 2017-11-30 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Combination therapy - combined map2k4/map3k1 and mek/erk inhibition |
AU2017339890A1 (en) * | 2016-10-05 | 2019-04-11 | Recurium Ip Holdings, Llc | Spirocyclic compounds |
GB201706327D0 (en) | 2017-04-20 | 2017-06-07 | Otsuka Pharma Co Ltd | A pharmaceutical compound |
AR117398A1 (en) | 2018-03-12 | 2021-08-04 | Abbvie Inc | INHIBITORS OF SIGNALING MEDIATED BY TYROSINE KINASE 2 |
CN114605329B (en) * | 2022-03-28 | 2024-01-26 | 河南中医药大学 | Substituted indazole carboxamides or substituted azaindazole carboxamides FLT3 inhibitors and uses thereof |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9213077D0 (en) | 1992-06-19 | 1992-08-05 | Erba Carlo Spa | Polymerbound taxol derivatives |
IL145757A (en) * | 2000-02-05 | 2007-12-03 | Vertex Pharma | Pyrazole derivatives and pharmaceutical compositions containing the same |
US6897231B2 (en) * | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
MY130778A (en) * | 2001-02-09 | 2007-07-31 | Vertex Pharma | Heterocyclic inhibitiors of erk2 and uses thereof |
JP4648703B2 (en) * | 2002-09-05 | 2011-03-09 | アベンティス・ファーマ・ソシエテ・アノニム | Novel aminoindazole derivatives as pharmaceuticals and pharmaceutical compositions containing them |
-
2006
- 2006-12-11 EP EP06845064A patent/EP1966151B1/en active Active
- 2006-12-11 RS RS20110516A patent/RS51981B/en unknown
- 2006-12-11 SI SI200631221T patent/SI1966151T1/en unknown
- 2006-12-11 DK DK06845064.2T patent/DK1966151T3/en active
- 2006-12-11 KR KR1020087016729A patent/KR101417136B1/en active IP Right Grant
- 2006-12-11 CN CN2006800527776A patent/CN101370784B/en active Active
- 2006-12-11 RU RU2008128119/04A patent/RU2442778C9/en active
- 2006-12-11 US US11/636,954 patent/US20070191604A1/en not_active Abandoned
- 2006-12-11 CA CA2633023A patent/CA2633023C/en active Active
- 2006-12-11 BR BRPI0619823A patent/BRPI0619823B8/en not_active IP Right Cessation
- 2006-12-11 JP JP2008545685A patent/JP4881957B2/en not_active Expired - Fee Related
- 2006-12-11 MY MYPI20082076A patent/MY149430A/en unknown
- 2006-12-11 PL PL06845064T patent/PL1966151T3/en unknown
- 2006-12-11 ES ES06845064T patent/ES2372976T3/en active Active
- 2006-12-11 NZ NZ569087A patent/NZ569087A/en not_active IP Right Cessation
- 2006-12-11 WO PCT/US2006/046959 patent/WO2007070398A1/en active Application Filing
- 2006-12-11 AU AU2006326616A patent/AU2006326616B2/en not_active Ceased
- 2006-12-11 PT PT06845064T patent/PT1966151E/en unknown
- 2006-12-11 AT AT06845064T patent/ATE527240T1/en active
- 2006-12-12 AR ARP060105474A patent/AR056891A1/en active IP Right Grant
- 2006-12-12 PE PE2010000279A patent/PE20100562A1/en not_active Application Discontinuation
- 2006-12-12 PE PE2006001592A patent/PE20071095A1/en active IP Right Grant
- 2006-12-12 TW TW095146375A patent/TWI344466B/en not_active IP Right Cessation
-
2008
- 2008-06-10 IL IL192034A patent/IL192034A/en active IP Right Grant
- 2008-06-13 EC EC2008008550A patent/ECSP088550A/en unknown
- 2008-06-24 ZA ZA200805525A patent/ZA200805525B/en unknown
- 2008-07-11 NO NO20083114A patent/NO341831B1/en not_active IP Right Cessation
- 2008-09-12 HK HK08110160.5A patent/HK1114851A1/en not_active IP Right Cessation
-
2011
- 2011-11-30 HR HR20110892T patent/HRP20110892T1/en unknown
-
2012
- 2012-01-04 CY CY20121100006T patent/CY1112760T1/en unknown
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PC | Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee) |
Effective date: 20221209 |